阴极
氧化还原
电化学
快离子导体
离子
材料科学
锂(药物)
扩散
电极
化学工程
化学物理
无机化学
化学
电解质
热力学
物理化学
医学
物理
有机化学
工程类
内分泌学
作者
Han Li,Yao Wang,Xudong Zhao,Junteng Jin,Qiuyu Shen,Jie Li,Yukun Liu,Xuanhui Qu,Lifang Jiao,Yongchang Liu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-08-04
卷期号:8 (9): 3666-3675
被引量:26
标识
DOI:10.1021/acsenergylett.3c01183
摘要
Natrium superionic conductor (NASICON)-type phosphates have attracted widespread attention as cathodes for sodium-ion batteries (SIBs) due to their 3D open frameworks facilitating Na+ diffusion, but they are characterized by mediocre energy density or rapid capacity decay. Herein, we delicately design a multielectron-reaction and low-strain Na3.5Fe0.5VCr0.5(PO4)3/C cathode material featuring a high working voltage (∼3.43 V), high reversible capacity (148.5 mAh g–1), and high cycling stability (95.1% capacity retention over 2000 cycles). The deviation in the reaction potential of each redox couple (Fe2+/Fe3+, V3+/V4+/V5+, and Cr3+/Cr4+) efficaciously alleviates the lattice strain accumulation, ensuring a small cell volume variation of 3.87% during the highly reversible charge–discharge processes, as confirmed by systematic in situ/ex situ analyses. Moreover, the fast reaction kinetics and the unexpected reversible Na1-ion (6b site) release/uptake are elucidated via multiple electrochemical characterizations and theoretical computations. This rational design strategy of incorporating versatile redox couples with different roles will broaden the horizons of high-performance NASICON-type cathodes.
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